Daytime Nighttime Kit
Product Images NDC 41226-778

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Daytime Nighttime (NDC 41226-778). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kroger Company, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

778t-kroger-day-48s-label (778t Kroger Day 48s Label)

The image shows a label for Kroger Health Daytime Cold & Flu Mini Softgels, containing acetaminophen, dextromethorphan HBr, and phenylephrine HCl. The package contains 48 softgels and is identified with UPC or NDC code 41226-777-48. The product is described as a pain reliever, fever reducer, cough suppressant, and nasal decongestant.*

FDA Label Image

778t-kroger-day-night-96s-ifc (778t Kroger Day Night 96s Ifc)

Packaging label for Kroger Health Daytime Nighttime Ultra Concentrated Cold & Flu Kit containing 96 total mini softgels. Includes 48 daytime softgels with acetaminophen, dextromethorphan HBr, and phenylephrine HCl for pain relief, cough suppression, and nasal decongestant. Includes 48 nighttime softgels with acetaminophen, dextromethorphan HBr, doxylamine succinate for pain relief, cough suppression, and antihistamine. Features detailed Drug Facts and usage directions.*

FDA Label Image

778t-kroger-night-48s-label (778t Kroger Night 48s Label)

Packaging label for Kroger Health NightTime Acetaminophen Cold & Flu 48 Mini Softgels. The label highlights the product as a pain reliever and fever reducer with active ingredients including acetaminophen, dextromethorphan HBr, and doxylamine succinate. The label displays the Kroger logo and states the product count as 48 softgels.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.